Enhance clinical research initiatives with Ocugen as a Clinical Research Associate. Focus on managing Phase 1-3 studies while ensuring regulatory compliance and participant protection. This role is based in Canada and plays a crucial part in overseeing the planning and execution of clinical trials.

In this capacity, you will coordinate operational activities, manage site interactions, and maintain comprehensive study documentation. An in-depth understanding of clinical research guidelines and practices is vital for this position. Key Responsibilities:

- Support all phases of clinical trial management
- Coordinate investigational site activities and training
- Maintain accurate CTMS and eTMF records
- Review study documentation for compliance and accuracy
- Track investigational products and documentation through all phases Requirements:
- Bachelor’s degree in life sciences, nursing, or equivalent
- Three years of hands-on clinical research experience
- Familiarity with ICH, GCP, and Canadian regulations
- Proficiency with eTMF and CTMS systems preferred
- Strong problem-solving and communication skills Leverage your expertise in clinical trials at Ocugen by ensuring protected and effective research practices.

📌 Ocugen Clinical Research Associate Position (Toronto)
🏢 OCUGEN OPCO
📍 Toronto